Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsm4 |
G |
T |
7: 119,292,933 (GRCm39) |
R21L |
probably benign |
Het |
Adgb |
T |
A |
10: 10,286,562 (GRCm39) |
R120* |
probably null |
Het |
Adgra3 |
C |
A |
5: 50,144,977 (GRCm39) |
A539S |
probably benign |
Het |
Ank2 |
A |
G |
3: 126,740,047 (GRCm39) |
S1946P |
unknown |
Het |
Card6 |
TTGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGCGGATGAGAGGGCTTAGCATGGGAGGACTG |
TTGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGCGGATGAGAGGGCTTAGCATGGGAGGACTG |
15: 5,128,173 (GRCm39) |
|
probably benign |
Het |
Cdc20b |
A |
T |
13: 113,173,582 (GRCm39) |
|
probably null |
Het |
Cfh |
T |
G |
1: 140,036,328 (GRCm39) |
D730A |
possibly damaging |
Het |
Dennd1a |
T |
C |
2: 37,748,444 (GRCm39) |
H345R |
probably damaging |
Het |
Dhx36 |
T |
C |
3: 62,388,294 (GRCm39) |
S614G |
possibly damaging |
Het |
Dio1 |
C |
T |
4: 107,149,583 (GRCm39) |
V240I |
possibly damaging |
Het |
Dnah12 |
A |
G |
14: 26,492,460 (GRCm39) |
D1200G |
probably benign |
Het |
Dpy19l4 |
A |
T |
4: 11,265,909 (GRCm39) |
S680T |
probably benign |
Het |
Eef2 |
CCC |
CCCC |
10: 81,014,602 (GRCm39) |
|
probably null |
Het |
Fcrlb |
T |
C |
1: 170,735,416 (GRCm39) |
|
probably null |
Het |
Gad1 |
T |
A |
2: 70,417,476 (GRCm39) |
I253K |
possibly damaging |
Het |
Gars1 |
A |
G |
6: 55,054,688 (GRCm39) |
D665G |
probably damaging |
Het |
Gldn |
A |
G |
9: 54,245,648 (GRCm39) |
T400A |
probably benign |
Het |
Gm1110 |
C |
A |
9: 26,795,122 (GRCm39) |
V455L |
possibly damaging |
Het |
Gm11444 |
A |
G |
11: 85,741,069 (GRCm39) |
V30A |
unknown |
Het |
Gm5134 |
T |
C |
10: 75,800,271 (GRCm39) |
S51P |
probably damaging |
Het |
Gprc6a |
C |
T |
10: 51,502,883 (GRCm39) |
A327T |
probably benign |
Het |
Gstt2 |
A |
T |
10: 75,670,019 (GRCm39) |
D34E |
probably benign |
Het |
Icam2 |
A |
G |
11: 106,271,589 (GRCm39) |
F78L |
probably damaging |
Het |
Jakmip1 |
T |
G |
5: 37,284,802 (GRCm39) |
C630G |
possibly damaging |
Het |
Kcnu1 |
A |
T |
8: 26,386,686 (GRCm39) |
N523I |
probably damaging |
Het |
Klf10 |
A |
G |
15: 38,297,282 (GRCm39) |
S253P |
probably benign |
Het |
Mmd2 |
A |
T |
5: 142,594,361 (GRCm39) |
M1K |
probably null |
Het |
Mroh2b |
G |
T |
15: 4,960,543 (GRCm39) |
G759C |
probably benign |
Het |
Or10w3 |
T |
C |
19: 13,704,465 (GRCm39) |
L280P |
probably damaging |
Het |
Or8k32 |
C |
T |
2: 86,368,872 (GRCm39) |
C127Y |
probably damaging |
Het |
Orc5 |
A |
G |
5: 22,755,197 (GRCm39) |
F22S |
possibly damaging |
Het |
Prlr |
A |
G |
15: 10,329,021 (GRCm39) |
I499V |
probably benign |
Het |
Ptbp1 |
A |
G |
10: 79,694,954 (GRCm39) |
N94S |
probably benign |
Het |
Rassf3 |
C |
A |
10: 121,312,103 (GRCm39) |
|
probably benign |
Het |
Rbm33 |
C |
T |
5: 28,573,264 (GRCm39) |
P455S |
probably damaging |
Het |
Sgcd |
C |
G |
11: 47,016,481 (GRCm39) |
G127A |
possibly damaging |
Het |
Slc22a13 |
A |
G |
9: 119,024,226 (GRCm39) |
I336T |
possibly damaging |
Het |
Slc25a31 |
A |
T |
3: 40,679,471 (GRCm39) |
D312V |
possibly damaging |
Het |
Slc37a4 |
G |
A |
9: 44,312,818 (GRCm39) |
S324N |
probably benign |
Het |
Slco1a5 |
A |
G |
6: 142,221,207 (GRCm39) |
V13A |
probably benign |
Het |
Srgap2 |
T |
C |
1: 131,220,371 (GRCm39) |
H907R |
probably damaging |
Het |
Supv3l1 |
A |
C |
10: 62,271,487 (GRCm39) |
V381G |
probably damaging |
Het |
Supv3l1 |
C |
A |
10: 62,271,488 (GRCm39) |
V381L |
possibly damaging |
Het |
Syne1 |
T |
C |
10: 5,299,324 (GRCm39) |
D977G |
probably damaging |
Het |
Syt3 |
T |
A |
7: 44,040,272 (GRCm39) |
Y168* |
probably null |
Het |
Tshz1 |
A |
T |
18: 84,032,790 (GRCm39) |
Y539* |
probably null |
Het |
Ttll13 |
A |
G |
7: 79,907,981 (GRCm39) |
K501R |
probably benign |
Het |
Ttn |
G |
A |
2: 76,612,732 (GRCm39) |
Q17116* |
probably null |
Het |
Vcan |
T |
C |
13: 89,840,577 (GRCm39) |
T1656A |
probably damaging |
Het |
Vmn1r73 |
G |
T |
7: 11,491,082 (GRCm39) |
C300F |
probably benign |
Het |
Vmn2r9 |
T |
C |
5: 108,992,948 (GRCm39) |
K521E |
probably damaging |
Het |
Zdhhc11 |
T |
A |
13: 74,130,885 (GRCm39) |
|
probably benign |
Het |
Zfp760 |
T |
C |
17: 21,941,907 (GRCm39) |
S361P |
possibly damaging |
Het |
Zranb2 |
A |
G |
3: 157,246,309 (GRCm39) |
Y114C |
probably damaging |
Het |
|
Other mutations in Or2b7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01593:Or2b7
|
APN |
13 |
21,739,389 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01866:Or2b7
|
APN |
13 |
21,739,343 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02289:Or2b7
|
APN |
13 |
21,739,758 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02350:Or2b7
|
APN |
13 |
21,739,772 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02357:Or2b7
|
APN |
13 |
21,739,772 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02793:Or2b7
|
APN |
13 |
21,740,172 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02875:Or2b7
|
APN |
13 |
21,740,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R0785:Or2b7
|
UTSW |
13 |
21,739,958 (GRCm39) |
missense |
probably benign |
0.02 |
R1773:Or2b7
|
UTSW |
13 |
21,739,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R3429:Or2b7
|
UTSW |
13 |
21,739,975 (GRCm39) |
nonsense |
probably null |
|
R3430:Or2b7
|
UTSW |
13 |
21,739,975 (GRCm39) |
nonsense |
probably null |
|
R4232:Or2b7
|
UTSW |
13 |
21,739,631 (GRCm39) |
missense |
probably damaging |
0.98 |
R4883:Or2b7
|
UTSW |
13 |
21,739,658 (GRCm39) |
missense |
probably benign |
0.22 |
R5586:Or2b7
|
UTSW |
13 |
21,739,266 (GRCm39) |
missense |
probably damaging |
1.00 |
R6032:Or2b7
|
UTSW |
13 |
21,740,077 (GRCm39) |
missense |
probably benign |
0.01 |
R6032:Or2b7
|
UTSW |
13 |
21,740,077 (GRCm39) |
missense |
probably benign |
0.01 |
R6542:Or2b7
|
UTSW |
13 |
21,739,677 (GRCm39) |
missense |
probably damaging |
0.99 |
R7014:Or2b7
|
UTSW |
13 |
21,740,108 (GRCm39) |
missense |
probably benign |
0.02 |
R7598:Or2b7
|
UTSW |
13 |
21,739,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R7982:Or2b7
|
UTSW |
13 |
21,740,136 (GRCm39) |
missense |
probably benign |
|
R8239:Or2b7
|
UTSW |
13 |
21,739,788 (GRCm39) |
missense |
probably benign |
0.01 |
R8339:Or2b7
|
UTSW |
13 |
21,739,996 (GRCm39) |
missense |
probably damaging |
0.99 |
R8698:Or2b7
|
UTSW |
13 |
21,739,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R8956:Or2b7
|
UTSW |
13 |
21,740,169 (GRCm39) |
missense |
probably benign |
0.00 |
R8977:Or2b7
|
UTSW |
13 |
21,740,016 (GRCm39) |
missense |
possibly damaging |
0.57 |
RF051:Or2b7
|
UTSW |
13 |
21,739,693 (GRCm39) |
frame shift |
probably null |
|
|